MODIFIED ROTATION AIR FLUIDIZED BED/THE THERAPULSE

MODIFIED ROTATION AIR FLUIDIZED BED/THE THERAPULSE is an FDA 510(k)-cleared medical device (K875321) manufactured by Kinetic Concepts, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 26, 1988. Regulation: 8.